117019-48-4

Upstream product

• 116927-04-9 Methyl (2E,6E,10S,11S)-3,7-Diethyl-10,11-isopropylidenedioxy-11-methyl-2,6-tridecadienoate 
• 116927-08-3 Methyl (2Z,6E,10S,11S)-7-Ethyl-10,11-isopropylidenedioxy-11-methyl-3-phenylthio-2,6-tridecadienoate 
• 17447-02-8 (2E,6E)-methyl 3-ethyl-7-methylnona-2,6-dienoate 
• 1389395-00-9 (2Z,6E)-methyl 3,7-bis(tosyloxy)octa-2,6-dienoate 
• 1389394-98-2 (E)-methyl 3-oxo-7-(tosyloxy)oct-6-enoate 
• 1389395-08-7 C₂₄H₃₄O₆S 
• 557-20-0 diethylzinc 
• 1389395-07-6 C₁₇H₂₈O₄ 
• 1389395-05-4 C₁₂H₂₂O₂ 
• 1389395-04-3 C₁₃H₂₂O₃ 
• 1389395-03-2 C₁₃H₂₄O₄ 
• 116927-09-4 Methyl (2E,6E,10S,11S)-3,7-Diethyl-10,11-dihydroxy-11-methyl-2,6-tridecadienoate 
• 116927-03-8 (2Z,6E)-3-(Diethoxy-phosphoryloxy)-7-ethyl-9-((4S,5S)-5-ethyl-2,2,5-trimethyl-[1,3]dioxolan-4-yl)-nona-2,6-dienoic acid methyl ester 
• 116927-11-8 (2E,6E)-(10S,11S)-3,7-Diethyl-11-hydroxy-10-methanesulfonyloxy-11-methyl-trideca-2,6-dienoic acid methyl ester 

Relevant academic research and scientific papers

Stereoselective total syntheses of insect juvenile hormones JH 0 and JH i

Total syntheses of juvenile hormones JH 0 and JH I have been achieved by a new iterative enol tosylate homologation strategy. Georg Thieme Verlag Stuttgart · New York.

Synthesis of Compounds with Juvenile Hormone Activity, XXVII. - Synthesis of Enantiomerically Pure (10R,11S)-(+)-Juvenile Hormone 0

The synthesis of (10R,11S)-(+)-juvenile hormone 0 (1) was achieved by employing an improved method for the construction of a trisubstituted double bond.